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Phosgene → 5-Nitro-1H-benzo[d][1,3]oxazine-2,4-dione

HRID 851639
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인쇄 미리보기

반응식

HRID 851639 반응식
Cl.[NH2:2][C:3]1[CH:11]=[CH:10][CH:9]=[C:8]([N+:12]([O-:14])=[O:13])[C:4]=1[C:5]([OH:7])=[O:6].[C:15](Cl)(Cl)=[O:16]>O.O1CCCC1>[N+:12]([C:8]1[CH:9]=[CH:10][CH:11]=[C:3]2[NH:2][C:15](=[O:16])[O:7][C:5](=[O:6])[C:4]=12)([O-:14])=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 6371Phosgene2회HCID 70531720HCID 70531720, 화합물

생성물 1

HCID 1347955-Nitro-1H-benzo[d][1,3]oxazine-2,4-dione

시약·촉매·용매 2

HCID 962Water용매2회HCID 8028Tetrahydrofuran용매

실험 절차

A solution of 56.5 g of 2-amino-6-nitrobenzoic acid hydrochloride in 200 ml of demineralized water and 200 ml of tetrahydrofuran is cooled to 10° while stirring and treated with phosgene at 10°-30° for 1 hour, a precipitate resulting. The mixture is subsequently diluted with 300 ml of demineralized water and air is conducted through the suspension vigorously for about 3 hours (until the sample is negative for phosgene). The precipitate is filtered off, washed with water and dried in vacuo over phosphorus pentoxide. There is obtained 6-nitroisatoic acid anhydride as beige crystals of m.p. 220°-222° (decomposition).

후처리

  1. customa precipitate resulting
  2. filtrationThe precipitate is filtered off
  3. washwashed with water
  4. dry with materialdried in vacuo over phosphorus pentoxide

출처 및 근거

ORD 기록
ord-e57fd57caacd4ac7a3b0cc650a98fca4
출처 데이터셋
uspto-grants-1983_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04386028

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